FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00613994258106 · Model: LST · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00613994258106
Version / Model
LST
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-06-19
Public Version
4
Public Version Date
2023-08-08
Public Version Status
Update
Public Device Record Key
7c722863-fbb0-4d76-920d-2dd95a76436a

Device Description

TAPE LST LEVEL DETECTOR MOUNT

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DWA Control, pump speed, cardiopulmonary bypass

GMDN Terms

Code Name
33317 Cardiopulmonary bypass system centrifugal pump drive unit

Identifiers

Type ID
Primary 00613994258106

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K070286 000
K150530 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Atmospheric Limitation of 700 hPa to 1060 hPa
Type
Storage Environment Humidity
Temperature Range
10 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-40 – 66 Degrees Celsius